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Glucuronidase β Polyclonal Antibody

说明书

BYab-02643

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
WB;IHC;IF;ELISA
分子量(DA)
78kD
免疫原
The antiserum was produced against synthesized peptide derived from human GUSB. AA range:321-370
特异性
Glucuronidase β Polyclonal Antibody detects endogenous levels of Glucuronidase β protein.
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
IHC-p: 100-300.WB: 1/500 - 1/2000. ELISA: 1/10000.. IF 1:50-200
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度
1 mg/ml
背景(Background)
This gene encodes a hydrolase that degrades glycosaminoglycans, including heparan sulfate, dermatan sulfate, and chondroitin-4,6-sulfate. The enzyme forms a homotetramer that is localized to the lysosome. Mutations in this gene result in mucopolysaccharidosis type VII. Alternative splicing results in multiple transcript variants. There are many pseudogenes of this locus in the human genome.[provided by RefSeq, May 2014],
功能
catalytic activity:A beta-D-glucuronoside + H(2)O = D-glucuronate + an alcohol.,disease:Defects in GUSB are the cause of mucopolysaccharidosis type 7 (MPS7) [MIM:253220]; also known as Sly syndrome. MPS7 is an autosomal recessive lysosomal storage disease characterized by inability to degrade glucuronic acid-containing glycosaminoglycans. The phenotype is highly variable, ranging from severe lethal hydrops fetalis to mild forms with survival into adulthood. Most patients with the intermediate phenotype show hepatomegaly, skeletal anomalies, coarse facies, and variable degrees of mental impairment.,disease:Mucopolysaccharidosis type 7 is associated with non-immune hydrops fetalis [MIM:236750]. Hydrops fetalis is a generalized edema of the fetus with fluid accumulation in the body cavities.,enzyme regulation:Inhibited by L-aspartic acid.,function:Plays an important role in the degradation
基因名称(Gene Name)
GUSB
蛋白名称
Beta-glucuronidase
简称
Glucuronidase β
其他名称
GUSB; Beta-glucuronidase; Beta-G1
Fields
>>Pentose and glucuronate interconversions;>>Ascorbate and aldarate metabolism;>>Glycosaminoglycan degradation;>>Porphyrin metabolism;>>Drug metabolism - other enzymes;>>Metabolic pathways;>>Biosynthesis of cofactors;>>Lysosome
人基因ID
2990
人蛋白质序列数据库
P08236
小鼠基因ID
110006
小鼠蛋白质序列数据库
P12265
大鼠基因ID
24434
大鼠蛋白质序列数据库
P06760
细胞定位
Lysosome.
组织表达
Colon,Fibroblast,Liver,Placenta,Plasma,
储存(Storage)
-20°C/1 year

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Glucuronidase β Polyclonal Antibody

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